1. By Dr Abiodun Mark Akanmode.
Tissue Repair. By
Dr Abiodun Mark Akanmode.

2. Introduction.
The body's ability to replace injured or dead cells and to repair tissues after inflammation is critical to survival.
When injurious agents damage cells and tissues, the host responds by setting in motion a series of events that serve to eliminate these agents, contain the damage, and prepare the surviving cells for replication.
The repair of tissue damage caused by surgical resection,wounds, and diverse types of chronic injury can be broadly separated into two processes, regeneration and healing. Regeneration results in restitution of lost tissues; healing may
restore original structures but involves collagen deposition and scar formation.

3. Cell cycle.
Cell-cycle landmarks. The figure shows the cell-cycle phases (G0 , G1 , G2 , S, and M), the location of the G1 restriction point, and the G1 /S and G2 /M cell-cycle checkpoints.
Cells from labile tissues such as the epidermis and the gastrointestinal tract may cycle continuously; stable cells such as hepatocytes are quiescent but can enter the cell cycle; permanent such as neurons and cardiac myocytes have lost the capacity to proliferate.

6. Epidermal Growth Factor (EGF) and Transforming Growth Factor-a (TGF-a).
These two factors belong to the EGF family and share a common receptor. EGF was discovered by its ability to cause precocious tooth eruption and eyelid opening in newborn mice. EGF is
mitogenic for a variety of epithelial cells, hepatocytes, and fibroblasts. It is widely distributed in tissue secretions and fluids, such as sweat, saliva, urine, and intestinal contents. In healing
wounds of the skin, EGF is produced by keratinocytes, macrophages, and other inflammatory cells that migrate into the area. EGF binds to a receptor (EGFR) with intrinsic tyrosine kinase
activity, triggering the signal transduction

7. Hepatocyte Growth Factor (HGF).
HGF was originally isolated from platelets and serum. Subsequent studies demonstrated that it is identical to a previously identified growth factor known as scatter factor (HGF is also referred to as HGF/scatter factor). It has mitogenic effects in most epithelial cells, including hepatocytes and cells of the biliary epithelium in the liver, and epithelial cells of the lungs,mammary gland, skin, and other tissues.
Besides its mitogenic effects, HGF acts as a morphogen in embryonic development and promotes cell scattering and migration.
This factor is produced by fibroblasts, endothelial cells, and liver nonparenchymal cells

8. Vascular endothelial growth factor.
VEGF is a family of peptides that includes VEGF-A (referred throughout as VEGF), VEGF-B, VEGF-C, VEGF-D, and placental growth factor.
VEGF is a potent inducer of blood vessel formation in early development (vasculogenesis) and has a central role in the growth of new blood vessels (angiogenesis) in adults .
It promotes angiogenesis in tumors,chronic inflammation, and healing of wounds

9. Platelet derived growth factor.
PDGF is a family of several closely related proteins, each consisting of two chains designated A and B. All three isoforms of PDGF (AA, AB, and BB) are secreted and are biologically active.
PDGF is stored in platelet a granules and is released on platelet activation. It can also be produced by a variety of other cells, including activated macrophages, endothelial cells, smooth muscle cells, and many tumor cells.
PDGF causes migration and proliferation of fibroblasts, smooth muscle cells, and monocytes, It also participates in the activation of hepatic stellate cells in the initial steps of liver fibrosis

10. Fibroblast growth factor.
This is a family of growth factors containing more than 10 members, of which acidic FGF (aFGF, or FGF-1) and basic FGF (bFGF, or FGF-2) are the best characterized. FGF-1 and FGF-2 are made by a variety of cells.
A large number of functions are attributed to FGFs, including the following:
• New blood vessel formation (angiogenesis): FGF-2, in particular, has the ability to induce the steps necessary for new blood vessel formation both in vivo and in vitro (see below).
• Wound repair: FGFs participate in macrophage, fibroblast, and endothelial cell migration in damaged tissues and migration of epithelium to form new epidermis.

11. FGF cont.
• Development: FGFs play a role in skeletal muscle development and in lung maturation. For example, FGF-6 and its receptor induce myoblast proliferation and suppress myocyte
differentiation, providing a supply of proliferating myocytes. FGF-2 is also thought to be involved in the generation of angioblasts during embryogenesis. FGF-1 and FGF-2 are
involved in the specification of the liver from endodermal cells.
• Hematopoiesis: FGFs have been implicated in the differentiation of specific lineages of blood cells and development of bone marrow stroma.

12. Cell signaling and growth.
SIGNALING MECHANISMS IN CELL GROWTH
All growth factors function by binding to specific receptors, which deliver signals to the target cells.
These signals have two general effects: (1) they stimulate the transcription of many genes that were silent in the resting cells, and (2) several of these genes regulate the entry of the cells into the cell cycle and their passage through the various stages of the cell cycle.

13. Cont’s.
Cell proliferation is a tightly regulated process that involves a large number of molecules and interrelated pathways.
The first event that initiates cell proliferation is, usually, the binding of a signaling molecule, the ligand, to a specific cell receptor

14. Autocrine signaling.
Autocrine signaling: Cells respond to the signaling molecules that they themselves secrete, thus establishing an autocrine loop.
Several polypeptide growth factors and cytokines act in this manner.
Autocrine growth regulation plays a role in liver regeneration, proliferation of antigen-stimulated lymphocytes, and the growth of some tumors.
Tumors frequently overproduce growth factors and their receptors, thus stimulating their own proliferation through an autocrine loop.

15. Paracrine signaling.
Paracrine signaling: One cell type produces the ligand, which then acts on adjacent target cells that express the appropriate receptors.
The responding cells are in close proximity to the ligand-producing cell and are generally of a different type.
Paracrine stimulation is common in connective tissue repair of healing wounds, in which a factor produced by one cell type (e.g., a macrophage) has its growth effect on adjacent cells (e.g., a fibroblast).
Paracrine signaling is also necessary for hepatocyte replication during liver regeneration .

16. Endocrine signaling.
Endocrine signaling: Hormones are synthesized by cells of endocrine organs and act on target cells distant from their site of synthesis, being usually carried by the blood.

21. Complications in Cutaneous wound healing.
Complications in wound healing can arise from abnormalities in any of the basic components of the repair process. These aberrations can be grouped into three general categories:
(1)deficient scar formation
(2) excessive formation of the repair components, and
(3) formation of contractures

22. Inadequate formation of scar tissue.
Inadequate formation of granulation tissue or assembly of a scar can lead to two types of complications: wound dehiscence and ulceration. Dehiscence or rupture of a wound is most common after abdominal surgery and is due to increased abdominal pressure.
This mechanical stress on the abdominal wound can be generated by vomiting, coughing, or ileus.
Wounds can ulcerate because of inadequate vascularization during healing

23. excessive formation of the repair components
Excessive formation of the components of the repair process can also complicate wound healing. Aberrations of growth may occur even in what may begin initially as normal wound healing.
The accumulation of excessive amounts of collagen may give rise to a raised scar known as a hypertrophic scar; if the scar tissue grows beyond the boundaries of the original wound and doesnot regress, it is called a keloid .
Keloid formation appears to be an individual predisposition, and for unknown reasons this aberration is somewhat more common in African-Americans. The mechanisms of keloid formation are still unknown

24. Keloids.

25. formation of contractures.
Contraction in the size of a wound is an important part of the normal healing process.
An exaggeration of this process is called a contracture and results in deformities of the wound and the surrounding tissues. Contractures are particularly prone to develop on the palms, the soles, and the anterior aspect of the thorax.
Contractures are commonly seen after serious burns and can compromise the movement of joints